Ongoing Electroencephalographic Rhythms Related to Exploratory Movements in Transgenic TASTPM Mice.


Journal

Journal of Alzheimer's disease : JAD
ISSN: 1875-8908
Titre abrégé: J Alzheimers Dis
Pays: Netherlands
ID NLM: 9814863

Informations de publication

Date de publication:
2020
Historique:
pubmed: 22 9 2020
medline: 21 9 2021
entrez: 21 9 2020
Statut: ppublish

Résumé

The European PharmaCog study (http://www.pharmacog.org) has reported a reduction in delta (1-6 Hz) electroencephalographic (EEG) power (density) during cage exploration (active condition) compared with quiet wakefulness (passive condition) in PDAPP mice (hAPP Indiana V717F mutation) modeling Alzheimer's disease (AD) amyloidosis and cognitive deficits. Here, we tested the reproducibility of that evidence in TASTPM mice (double mutation in APP KM670/671NL and PSEN1 M146V), which develop brain amyloidosis and cognitive deficits over aging. The reliability of that evidence was examined in four research centers of the PharmaCog study. Ongoing EEG rhythms were recorded from a frontoparietal bipolar channel in 29 TASTPM and 58 matched "wild type" C57 mice (range of age: 12-24 months). Normalized EEG power was calculated. Frequency and amplitude of individual delta and theta frequency (IDF and ITF) peaks were considered during the passive and active conditions. Compared with the "wild type" group, the TASTPM group showed a significantly lower reduction in IDF power during the active over the passive condition (p < 0.05). This effect was observed in 3 out of 4 EEG recording units. TASTPM mice were characterized by "poor reactivity" of delta EEG rhythms during the cage exploration in line with previous evidence in PDAPP mice. The reliability of that result across the centers was moderate, thus unveiling pros and cons of multicenter preclinical EEG trials in TASTPM mice useful for planning future studies.

Sections du résumé

BACKGROUND
The European PharmaCog study (http://www.pharmacog.org) has reported a reduction in delta (1-6 Hz) electroencephalographic (EEG) power (density) during cage exploration (active condition) compared with quiet wakefulness (passive condition) in PDAPP mice (hAPP Indiana V717F mutation) modeling Alzheimer's disease (AD) amyloidosis and cognitive deficits.
OBJECTIVE
Here, we tested the reproducibility of that evidence in TASTPM mice (double mutation in APP KM670/671NL and PSEN1 M146V), which develop brain amyloidosis and cognitive deficits over aging. The reliability of that evidence was examined in four research centers of the PharmaCog study.
METHODS
Ongoing EEG rhythms were recorded from a frontoparietal bipolar channel in 29 TASTPM and 58 matched "wild type" C57 mice (range of age: 12-24 months). Normalized EEG power was calculated. Frequency and amplitude of individual delta and theta frequency (IDF and ITF) peaks were considered during the passive and active conditions.
RESULTS
Compared with the "wild type" group, the TASTPM group showed a significantly lower reduction in IDF power during the active over the passive condition (p < 0.05). This effect was observed in 3 out of 4 EEG recording units.
CONCLUSION
TASTPM mice were characterized by "poor reactivity" of delta EEG rhythms during the cage exploration in line with previous evidence in PDAPP mice. The reliability of that result across the centers was moderate, thus unveiling pros and cons of multicenter preclinical EEG trials in TASTPM mice useful for planning future studies.

Identifiants

pubmed: 32955458
pii: JAD190351
doi: 10.3233/JAD-190351
doi:

Substances chimiques

Amyloid beta-Protein Precursor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

291-308

Auteurs

Claudio Del Percio (C)

Department of Physiology and Pharmacology "V Erspamer", Sapienza University of Rome, Rome, Italy.

Wilhelmus Drinkenburg (W)

Janssen Research and Development, Pharmaceutical Companies of J&J, Beerse, Belgium.

Susanna Lopez (S)

Department of Physiology and Pharmacology "V Erspamer", Sapienza University of Rome, Rome, Italy.
Department of Emergency and Organ Transplantation - Nephrology, Dialysis and Transplantation Unit, Aldo Moro University of Bari, Bari, Italy.

Maria Teresa Pascarelli (MT)

Oasi Research Institute - IRCCS, Troina, Italy.

Roberta Lizio (R)

IRCCS SDN, Naples, Italy.

Giuseppe Noce (G)

IRCCS SDN, Naples, Italy.

Raffaele Ferri (R)

Oasi Research Institute - IRCCS, Troina, Italy.

Jesper Frank Bastlund (JF)

H. Lundbeck A/S, Valby, Denmark.

Bettina Laursen (B)

H. Lundbeck A/S, Valby, Denmark.

Ditte Zerlang Christensen (DZ)

H. Lundbeck A/S, Valby, Denmark.

Jan T Pedersen (JT)

H. Lundbeck A/S, Valby, Denmark.

Gianluigi Forloni (G)

Department of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Angelisa Frasca (A)

Department of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Francesco M Noè (FM)

Department of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Paolo Francesco Fabene (PF)

Department of Neurological Biomedical and Movement Sciences, University of Verona, Verona, Italy.

Giuseppe Bertini (G)

Department of Neurological Biomedical and Movement Sciences, University of Verona, Verona, Italy.

Valeria Colavito (V)

Department of Neurological Biomedical and Movement Sciences, University of Verona, Verona, Italy.

Marina Bentivoglio (M)

Department of Neurological Biomedical and Movement Sciences, University of Verona, Verona, Italy.

Jonathan Kelley (J)

Janssen Research and Development, Pharmaceutical Companies of J&J, Beerse, Belgium.

Sophie Dix (S)

Eli Lilly, Erl Wood Manor, Windlesham, Surrey, UK.

Francesco Infarinato (F)

IRCCS San Raffaele Pisana, Rome, Italy.

Andrea Soricelli (A)

IRCCS SDN, Naples, Italy.
Department of Motor Sciences and Healthiness, University of Naples Parthenope, Naples, Italy.

Fabrizio Stocchi (F)

Institute for Research and Medical Care, IRCCS San Raffaele Pisana, Roma, Italy.

Jill C Richardson (JC)

GlaxoSmithKline R&D Neurotherapeutics Area UK, Gunnels Wood Road, Stevenage, Hertfordshire, UK.

Claudio Babiloni (C)

Department of Physiology and Pharmacology "V Erspamer", Sapienza University of Rome, Rome, Italy.
San Raffaele Cassino, Cassino (FR), Italy.

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